Endo-Therapeutics, Inc. recalls eSuction Small Cavity, Model ET2005
- Recall date
- October 24, 2022
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0270-2023
- FDA classification
- Class II
- Brand / firm
- Endo-Therapeutics, Inc.
- Sold / distributed
- US distribution to Florida and Pennsylvania
Why it was recalled
Improper device regulatory classification
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
eSuction Small Cavity, Model ET2005
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